FMRP Enhances the Translation of 4EBP2 mRNA during Neuronal Differentiation

FMRP is a multifunctional protein encoded by the Fragile X Messenger Ribonucleoprotein 1 gene (FMR1). The inactivation of the FMR1 gene results in fragile X syndrome (FXS), a serious neurodevelopmental disorder. FMRP deficiency causes abnormal neurite outgrowth, which is likely to lead to abnormal l...

Descripción completa

Detalles Bibliográficos
Autores principales: Yu, Jinbae, Woo, Youngsik, Kim, Heesun, An, Sihyeon, Park, Sang Ki, Jang, Sung Key
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671300/
https://www.ncbi.nlm.nih.gov/pubmed/38003508
http://dx.doi.org/10.3390/ijms242216319

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10671300/
https://www.ncbi.nlm.nih.gov/pubmed/38003508
http://dx.doi.org/10.3390/ijms242216319

Ejemplares similares